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Rare genetic variants involved in increased risk of paroxysmal atrial fibrillation in a Japanese population
Tabata, Kanji, Sudo, Takeaki, Nagata, Yuki, Ihara, Kensuke, Asada, Ken, Kinoshita, Atsuhiro, Tanaka, Yasuaki, Yamauchi, Yasuteru, Sasaki, Takeshi, Hachiya, Hitoshi, Imai, Yasushi, Fujita, Hideo, Sasano, Tetsuo, Furukawa, Tetsushi, Iwata, Takanori, Tanaka, Toshihiro
Published in Scientific reports (17.04.2025)
Published in Scientific reports (17.04.2025)
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Journal Article
Occurrence of Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations in Patients with Allergic Bronchopulmonary Aspergillosis Complicating Asthma
Kanaujia, Rimjhim, Arora, Amit, Chakrabarti, Arunaloke, Rudramurthy, Shivaprakash M., Agarwal, Ritesh
Published in Mycopathologia (1975) (01.06.2022)
Published in Mycopathologia (1975) (01.06.2022)
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Journal Article
Low-Frequency IL23R Coding Variant Associated with Crohn’s Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis
Onodera, Kei, Arimura, Yoshiaki, Isshiki, Hiroyuki, Kawakami, Kentaro, Nagaishi, Kanna, Yamashita, Kentaro, Yamamoto, Eiichiro, Niinuma, Takeshi, Naishiro, Yasuyoshi, Suzuki, Hiromu, Imai, Kohzoh, Shinomura, Yasuhisa
Published in PloS one (16.09.2015)
Published in PloS one (16.09.2015)
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Journal Article
Peripheral blood microbial signatures in current and former smokers
Morrow, Jarrett D., Castaldi, Peter J., Chase, Robert P., Yun, Jeong H., Lee, Sool, Liu, Yang-Yu, Hersh, Craig P.
Published in Scientific reports (06.10.2021)
Published in Scientific reports (06.10.2021)
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Journal Article
Whole genome sequencing of 10K patients with acute ischaemic stroke or transient ischaemic attack: design, methods and baseline patient characteristics
Cheng, Si, Xu, Zhe, Liu, Yang, Lin, Jinxi, Jiang, Yong, Wang, Yilong, Meng, Xia, Wang, Anxin, Huang, Xinying, Wang, Zhimin, Chen, Guohua, Wu, Songdi, Jia, Zhengchang, Chen, Yongming, Qiu, Xuerong, Wu, Jun, Song, Binbin, Ji, Weizhong, An, Zhongping, Xue, Wenjun, Zhao, Lili, Geng, Yu, Li, Hongyan, Li, Hao, Wang, Yongjun
Published in Stroke and vascular neurology (01.06.2021)
Published in Stroke and vascular neurology (01.06.2021)
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Journal Article
No interaction between polygenic scores and childhood trauma in predicting suicide attempt in schizophrenia
Bani-Fatemi, Ali, Tasmim, Samia, Wang, Kevin Z, Warsh, Jerry, Sibille, Etienne, De Luca, Vincenzo
Published in Progress in neuro-psychopharmacology & biological psychiatry (08.03.2019)
Published in Progress in neuro-psychopharmacology & biological psychiatry (08.03.2019)
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Journal Article
Validation and assessment of variant calling pipelines for next-generation sequencing
Pirooznia, Mehdi, Kramer, Melissa, Parla, Jennifer, Goes, Fernando S, Potash, James B, McCombie, W Richard, Zandi, Peter P
Published in Human genomics (30.07.2014)
Published in Human genomics (30.07.2014)
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Journal Article
Evidence for Association Between Low Frequency Variants in CHRNA6/CHRNB3 and Antisocial Drug Dependence
Kamens, Helen M., Corley, Robin P., Richmond, Phillip A., Darlington, Todd M., Dowell, Robin, Hopfer, Christian J., Stallings, Michael C., Hewitt, John K., Brown, Sandra A., Ehringer, Marissa A.
Published in Behavior genetics (01.09.2016)
Published in Behavior genetics (01.09.2016)
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Journal Article
Detailed comparison of two popular variant calling packages for exome and targeted exon studies
Warden, Charles D., Adamson, Aaron W., Neuhausen, Susan L., Wu, Xiwei
Published in PeerJ (San Francisco, CA) (30.09.2014)
Published in PeerJ (San Francisco, CA) (30.09.2014)
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Journal Article
tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine
Gillies, Christopher E., Otto, Edgar A., Vega-Warner, Virginia, Robertson, Catherine C., Sanna-Cherchi, Simone, Gharavi, Ali, Crawford, Brendan, Bhimma, Rajendra, Winkler, Cheryl, Kang, Hyun Min, Sampson, Matthew G.
Published in BMC bioinformatics (10.06.2016)
Published in BMC bioinformatics (10.06.2016)
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Journal Article
Whole-Exome Sequencing in Multiplex Families to Identify Novel AYA Classical Hodgkin Lymphoma Predisposition Genes
Xu, Keren, Wadé, Niquelle B, Hwang, Amie E., Conti, David V, Salehi, Maryam, Mack, Thomas M, Cortessis, Victoria, Van Den Berg, David J, de Smith, Adam J., Cozen, Wendy
Published in Blood (23.11.2021)
Published in Blood (23.11.2021)
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Journal Article
CT-018: Germline Immune Genetics Influencing CAR-T Therapy Response in Patients With Aggressive B-Cell Lymphoma
Oñate, Sara Fernández de Córdoba, Sebastián, Ismael de la Iglesia San, García, María Martínez, Alcoceba, Miguel, Alvarez, María Garcia, Bailén, Rebeca, Chicano, María, Martín, Ana África, Kwon, Mi, Oreiro, Mariana Bastos, Anguita, Javier, Olmos, Pablo Martínez, Gallardo, David, Laperche, Carolina Martínez, Borde, Ismael Buño
Published in Clinical lymphoma, myeloma and leukemia (01.09.2025)
Published in Clinical lymphoma, myeloma and leukemia (01.09.2025)
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Journal Article
Abstract 5232: Using an integrated gene-based sequence kernel association test (intSKAT) to identify subtype specific single nucleotide variants in glioma
Chen, Yian Ann, Teer, Jamie K., Thompson, Zachary J., Baskin, Rebekah L., Zhang, Yonghong O., Fisher, Kate J., Chen, Zhihua, Monteiro, Alvaro N., Egan, Kathleen M.
Published in Cancer research (Chicago, Ill.) (15.07.2016)
Published in Cancer research (Chicago, Ill.) (15.07.2016)
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Journal Article
Abstract 4163: Genomic variation in PDAC-predisposing genes identified using the MCW germline exome panel
Abrudan, Jenica, Tsai, Susan, Demos, Wendy, Zimmermann, Michael T., Tschannen, Michael, Geurts, Jennifer, Mathison, Angela, Lomberk, Gwen, Evans, Douglas, Urrutia, Raul
Published in Cancer research (Chicago, Ill.) (01.07.2019)
Published in Cancer research (Chicago, Ill.) (01.07.2019)
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Journal Article
An investigation of obesity susceptibility genes in Northern Han Chinese by targeted resequencing
Wu, Yili, Wang, Weijing, Jiang, Wenjie, Yao, Jie, Zhang, Dongfeng
Published in Medicine (Baltimore) (01.02.2017)
Published in Medicine (Baltimore) (01.02.2017)
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Journal Article
Exome Sequencing in Chronic Lymphocytic Leukemia (CLL) and Multiple Myeloma (MM) Families Identifies Cosegregating Functional Variants
Beiggi, Sara, O’Brien, Daniel R, Achenbach, Sara J, Rabe, Kari G, Call, Timothy G, Kay, Neil E, Shanafelt, Tait D, Norman, Aaron D, Cunningham, Julie M, Rajkumar, Vincent, Kumar, Shaji, Cerhan, James R, Vachon, Celine M, Slager, Susan L
Published in Blood (06.12.2014)
Published in Blood (06.12.2014)
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Journal Article
Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease
Stone, Edwin M., Andorf, Jeaneen L., Whitmore, S. Scott, DeLuca, Adam P., Giacalone, Joseph C., Streb, Luan M., Braun, Terry A., Mullins, Robert F., Scheetz, Todd E., Sheffield, Val C., Tucker, Budd A.
Published in Ophthalmology (Rochester, Minn.) (01.09.2017)
Published in Ophthalmology (Rochester, Minn.) (01.09.2017)
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Journal Article
Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis: e0137801
Onodera, Kei, Arimura, Yoshiaki, Isshiki, Hiroyuki, Kawakami, Kentaro, Nagaishi, Kanna, Yamashita, Kentaro, Yamamoto, Eiichiro, Niinuma, Takeshi, Naishiro, Yasuyoshi, Suzuki, Hiromu
Published in PloS one (01.09.2015)
Published in PloS one (01.09.2015)
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Journal Article